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Home  > 5-chloro-1-benzothiophene-3-sulfonyl chloride

AV44082

1158208-47-9 | 5-chloro-1-benzothiophene-3-sulfonyl chloride

Packsize Purity Availability Price Discounted Price    Quantity
50mg 95% 1 week $359.00 $251.00 -   +
100mg 95% 1 week $511.00 $358.00 -   +
250mg 95% 1 week $709.00 $497.00 -   +
500mg 95% 1 week $1,090.00 $763.00 -   +
1g 95% 1 week $1,380.00 $966.00 -   +
2.5g 95% 1 week $2,660.00 $1,862.00 -   +
5g 95% 1 week $3,909.00 $2,737.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AV44082
Chemical Name: 5-chloro-1-benzothiophene-3-sulfonyl chloride
CAS Number: 1158208-47-9
Molecular Formula: C8H4Cl2O2S2
Molecular Weight: 267.1522
MDL Number: MFCD22391910
SMILES: Clc1ccc2c(c1)c(cs2)S(=O)(=O)Cl

 

Upstream Synthesis Route
  • 5-Chloro-1-benzothiophene-3-sulfonyl Chloride is a versatile chemical reagent widely used in organic synthesis due to its unique properties and reactivity. This compound plays a crucial role in various chemical reactions, especially in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its ability to introduce a sulfonyl chloride group onto aromatic compounds makes it a valuable building block in the production of complex organic molecules.In chemical synthesis, 5-Chloro-1-benzothiophene-3-sulfonyl Chloride is commonly employed as a sulfonylating agent, enabling the introduction of the sulfonyl group onto nucleophilic substrates. The sulfonyl chloride functional group is a powerful electrophile that can participate in reactions such as nucleophilic substitution, arylation, and cyclization, leading to the formation of new carbon-sulfur bonds. This reactivity makes 5-Chloro-1-benzothiophene-3-sulfonyl Chloride a key intermediate in the preparation of various sulfur-containing compounds with diverse applications.Furthermore, the presence of the chlorine atom in the benzothiophene ring confers additional synthetic versatility, allowing for further functionalization of the molecule through substitution or elimination reactions. By judiciously controlling the reaction conditions and selectivity, chemists can harness the reactivity of 5-Chloro-1-benzothiophene-3-sulfonyl Chloride to access a wide array of structurally intricate compounds with tailored properties.Overall, 5-Chloro-1-benzothiophene-3-sulfonyl Chloride serves as a valuable tool in the hands of synthetic chemists, enabling the construction of complex molecular architectures with precision and efficiency. Its utility in chemical synthesis extends across various industries, driving innovation and advancement in the field of organic chemistry.
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